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ferrocenecarboxylic acid

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Identification
Molecular formula
C10H10FeO2
CAS number
794-16-1
IUPAC name
iron(2+) 2,4-cyclopentadien-1-ylidenebut-1-en-1-yl radical 2-carboxyoxide radical
State
State
At room temperature, ferrocenecarboxylic acid is in a solid state, typically forming orange crystals.
Melting point (Celsius)
173.50
Melting point (Kelvin)
446.65
Boiling point (Celsius)
249.60
Boiling point (Kelvin)
522.75
General information
Molecular weight
186.03g/mol
Molar mass
186.0310g/mol
Density
1.5700g/cm3
Appearence
Ferrocene is characterized by its orange crystalline appearance. It is stable at room temperature and has a distinctive metal-organic scent.
Comment on solubility

Solubility of Iron(2+) 2,4-Cyclopentadien-1-ylidenebut-1-en-1-yl Radical 2-Carboxyoxide Radical

The solubility of a compound often provides crucial insights into its potential applications and reactivity. In the case of iron(2+) 2,4-cyclopentadien-1-ylidenebut-1-en-1-yl radical 2-carboxyoxide radical, there are several factors that may influence its solubility:

  • Polarity: The presence of carboxylic acid groups typically increases solubility in polar solvents, which can enhance the compound's dissolution in aqueous environments.
  • Coordination with Metals: The Fe ions may interact with solvents, affecting solubility through coordination dynamics.
  • Hydrogen Bonding: The presence of functional groups capable of hydrogen bonding can promote solubility in water.
  • Molecular Structure: The bulky cyclopentadienyl moiety may hinder solubility in certain organic solvents due to steric factors.

Overall, while predictions of solubility can be made based on chemical structure and functional groups, solubility testing is essential for precisely determining the behavior of this compound in various solvent systems. As a general rule, understanding the interactions between organic radicals and the solvent can lead to valuable insights into their solubility profiles.

Interesting facts

Interesting Facts About Iron(II) 2,4-Cyclopentadien-1-ylidenebut-1-en-1-yl Radical 2-Carboxyoxide Radical

The fascinating world of organometallic chemistry presents us with the intriguing compound Iron(II) 2,4-cyclopentadien-1-ylidenebut-1-en-1-yl radical 2-carboxyoxide radical. Here are some engaging insights about this unique compound:

  • Organometallic Marvel: This compound showcases the unique interaction between iron, a transition metal, and organic radicals, demonstrating the versatility of organometallic chemistry.
  • Structure and Stability: The presence of both cyclopentadienyl and enyl groups contributes to the compound's stability. These structures are known for their resonance, allowing for effective electron delocalization.
  • Reactivity: As a radical, this compound is expected to exhibit high reactivity. Radicals play crucial roles in many chemical reactions, particularly in organic synthesis, polymerization, and in biological systems.
  • Potential Applications: Compounds like this one are of interest in materials science, particularly in the production of polymers and in catalysis. Their properties can be harnessed for innovative applications in nanotechnology and electronics.
  • Research Significance: The study of iron-based radicals can give insights into *catalytic processes*, aiming for sustainable chemistry practices. Researchers are keenly interested in how such radicals can enable more efficient and environmentally-friendly chemical transformations.

In conclusion, the Iron(II) 2,4-cyclopentadien-1-ylidenebut-1-en-1-yl radical 2-carboxyoxide radical not only exemplifies the complexity of organometallic structures but also opens doors to exciting research opportunities and practical applications in various fields of chemistry.

Synonyms
(eta-1,3-Butadiene)tricarbonyliron
EINECS 235-140-3
Iron, (eta4-1,3-butadiene)tricarbonyl-, stereoisomer